Senior Clinical Research Associate II – Oncology
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Job Description
Oncology Sr. CRA 2 responsible for all aspects of study site monitoring. Ensuring adherence to protocols and maintaining integrity of trial data with considerable travel involved.
Responsibilities:
- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites
- Conduct pre-study and initiation visits
- Ensure study staff have proper materials and instructions
- Verify informed consent procedures and protocol adherence
- Monitor data for missing or implausible data
Requirements:
- University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
- 5+ years of Clinical Monitoring experience
- Oncology experience, early phase preferred
- 30-50% overnight travel
Benefits:
- Health insurance
- 401(k)
- Paid time off
- Remote work options
- Professional development
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